Glycemic Emergency Management (GEM); An App for Rapid Response to Hypoglycemic and Hyperglycemic Situations

NCT ID: NCT02336217

Last Updated: 2025-05-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-09-30

Study Completion Date

2026-06-30

Brief Summary

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The purpose of this pilot study is to determine the utility of an algorithm for better glucose control in diabetic patients communicated via an App to help improve outcomes and reduce urgent care and ER visits as well as improve A1C and quality of life.

Detailed Description

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The aim of the study is to determine the impact of GEM (glycemic emergency management device-app) in reducing the frequency and severity of hypoglycemia episodes in persons with diabetes. Other objectives include: to determine whether the GEM system leads to improved glucose control (as measured by HbA1c) during participation in the pilot, to determine whether the GEM can be used as a cost effective solution in reducing ER and urgent care visits, to determine the difference in ADDQOL scores between persons with a functioning GEM system and those with a placebo device. The Study hypothesis is as follows: There wil be significant differences in number of hypoglycemic events, ER and urgent care visits, A1C, as well as quality of life as measured by the ADDQOL scores between persons with diabetes who have the functioning GEM device in their smart phones and those that do not have such a device installed in their smart phones.

The purpose of this pilot study is to determine the utility of this application to help improve outcomes and reduce urgent care and ER visits as well as improve A1C and quality of life in persons with diabetes. This approach may be a paradigm shift in the rapidly detecting, monitoring, intervening and managing the acute diabetic complications of hypoglycemia, hyperglycemia and diabetic ketoacidosis. Spiraling health care costs are a major concern to the economy of the US. New measures have been introduced in the Affordable Care Act to improve the efficiency of the health care delivery system. There is more emphasis on preventive health care services. Our study is a step in that direction since it utilizes existing smart phone technology and converts it into a medical device which can be of invaluable help to the patient.

Conditions

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Diabetes Mellitus

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Functioning App

These subjects have the complete algorithm functioning and communicated via the App.

Group Type EXPERIMENTAL

Experimental Group instructions for glucose management via App

Intervention Type OTHER

The Experimental Group receives individually calculated instructions for glucose management management via the App.

Non-functioning App

These subjects receive routine instructions via the App but not the complete algorithm.

Group Type PLACEBO_COMPARATOR

Placebo Comparator general instructions

Intervention Type OTHER

The Placebo Comparator Group receives general instructions but not the complete management algorithm

Interventions

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Experimental Group instructions for glucose management via App

The Experimental Group receives individually calculated instructions for glucose management management via the App.

Intervention Type OTHER

Placebo Comparator general instructions

The Placebo Comparator Group receives general instructions but not the complete management algorithm

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Type 1 or type 2 diabetes on therapeutic treatment other than just lifestyle changes
* Treatment by Marshall Internal Medicine Department
* Have a smart phone
* At least 6th grade education level

Exclusion Criteria

* Pregnant women
* Cognitive impairment
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Marshall University

OTHER

Sponsor Role lead

Responsible Party

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Henry Driscoll, MD

Chief, section of Endocrinology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Marshall Health

Huntington, West Virginia, United States

Site Status

Countries

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United States

Other Identifiers

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574049

Identifier Type: -

Identifier Source: org_study_id

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